A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258167



Internal ID21399875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39821140..40014081hg38UCSC Ensembl
chr9:41966158..42159099hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38192942
hg19192942
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730044
Supporting Variants
SamplesNA19238
Known GenesKGFLP2, LOC643648
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258167
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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